ID

34155

Beschreibung

Contrast-Enhanced Digital Mammography (CEDM) for Identifying a Change in Management of Women With Newly Diagnosed Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01303419

Link

https://clinicaltrials.gov/show/NCT01303419

Stichworte

  1. 14.01.19 14.01.19 -
Rechteinhaber

see on clinicaltrials.gov

Hochgeladen am

14. Januar 2019

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT01303419

Eligibility Breast Cancer NCT01303419

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
woman 21 years of age or older
Beschreibung

ID.1

Datentyp

boolean

the subject is able and willing to comply with study procedures and signed and dated informed consent is obtained.
Beschreibung

ID.2

Datentyp

boolean

newly diagnosed with breast cancer (dcis or invasive) identified through core biopsy or fine-needle aspiration (fna) within last 30 days.
Beschreibung

ID.3

Datentyp

boolean

will have or have had a bilateral ce-bmri performed within 30 days after the new breast cancer diagnosis.
Beschreibung

ID.4

Datentyp

boolean

Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
woman who has already had a lumpectomy for the index lesion.
Beschreibung

ID.5

Datentyp

boolean

woman undergoing neoadjuvant chemotherapy treatment, hormone treatment or radiation therapy.
Beschreibung

ID.6

Datentyp

boolean

woman who is pregnant or who believe she may be pregnant.
Beschreibung

ID.7

Datentyp

boolean

woman who has breast implant.
Beschreibung

ID.8

Datentyp

boolean

woman who has a contraindication to the intravenous use of iodinated or gadolinium-chelated contrast agent (e.g., allergy to either agent or severely impaired renal function).
Beschreibung

ID.9

Datentyp

boolean

Ähnliche Modelle

Eligibility Breast Cancer NCT01303419

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
woman 21 years of age or older
boolean
ID.2
Item
the subject is able and willing to comply with study procedures and signed and dated informed consent is obtained.
boolean
ID.3
Item
newly diagnosed with breast cancer (dcis or invasive) identified through core biopsy or fine-needle aspiration (fna) within last 30 days.
boolean
ID.4
Item
will have or have had a bilateral ce-bmri performed within 30 days after the new breast cancer diagnosis.
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
woman who has already had a lumpectomy for the index lesion.
boolean
ID.6
Item
woman undergoing neoadjuvant chemotherapy treatment, hormone treatment or radiation therapy.
boolean
ID.7
Item
woman who is pregnant or who believe she may be pregnant.
boolean
ID.8
Item
woman who has breast implant.
boolean
ID.9
Item
woman who has a contraindication to the intravenous use of iodinated or gadolinium-chelated contrast agent (e.g., allergy to either agent or severely impaired renal function).
boolean

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